HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599360Generated: October 25, 2026
Ethyl Acetoacetate → 4-(2-Ethoxycarbonyl-3-oxobutyl)biphenyl
https://huagongshe.com/reaction/1599360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 4-Phenylbenzyl chloride | HCID 15463 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-Ethoxycarbonyl-3-oxobutyl)biphenyl | HCID 13323701 | 95.4% |
Reaction Steps
In a four-necked flask equipped with a thermometer, dropping funnel and stirrer were placed 179 g (1.375 moles) of ethyl acetoacetate and 500 ml of ethanol, and then 31.5 g (1.375 moles) of sodium was added in portions thereto to form a solution. Then, a solution of 253.5 g (1.25 moles) of 4-chloromethylbiphenyl in 1000 ml of ethanol was added dropwise to the above solution at room temperature over a period of 2 hours. After completion of the addition, the resulting mixture was brought up to 65° C. and stirred at the temperature for 6 hours. After completion of the reaction ethanol was distilled off under reduced pressure, the residue obtained was extracted by addition of 1500 ml of toluene, and the organic layer was separated. The organic layer was washed with 10% hydrochloric acid, water, 5% aqueous sodium bicarbonate solution and water in said order and then concentrated under reduced pressure to obtain 353.5 g of 4-(2-ethoxycarbonyl-3-oxobutyl)biphenyl as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05741438 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-b21472884f8c45c083b37dd039c8d804 |
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| Source note | uspto-grants-1998_04 |
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